Linked Life Data

16188589

Source:http://linkedlifedata.com/resource/pubmed/id/16188589

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2005-9-28
pubmed:abstractText
Mutations in the RyR2-encoded cardiac ryanodine receptor/calcium release channel cause type 1 catecholaminergic polymorphic ventricular tachycardia (CPVT1).
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1547-5271
pubmed:author
pubmed:issnType
Print
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1099-105
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:16188589-Adolescent, pubmed-meshheading:16188589-Adult, pubmed-meshheading:16188589-Alleles, pubmed-meshheading:16188589-Child, pubmed-meshheading:16188589-Cohort Studies, pubmed-meshheading:16188589-Death, Sudden, Cardiac, pubmed-meshheading:16188589-Exercise Test, pubmed-meshheading:16188589-Family Health, pubmed-meshheading:16188589-Female, pubmed-meshheading:16188589-Gene Frequency, pubmed-meshheading:16188589-Genetic Predisposition to Disease, pubmed-meshheading:16188589-Genetic Testing, pubmed-meshheading:16188589-Genotype, pubmed-meshheading:16188589-Humans, pubmed-meshheading:16188589-Long QT Syndrome, pubmed-meshheading:16188589-Male, pubmed-meshheading:16188589-Middle Aged, pubmed-meshheading:16188589-Mutation, Missense, pubmed-meshheading:16188589-Myocardial Contraction, pubmed-meshheading:16188589-Phenotype, pubmed-meshheading:16188589-Polymorphism, Genetic, pubmed-meshheading:16188589-Referral and Consultation, pubmed-meshheading:16188589-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:16188589-Tachycardia, Ventricular, pubmed-meshheading:16188589-Ventricular Fibrillation
pubmed:year
2005
pubmed:articleTitle
Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.
pubmed:affiliation
Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural